Apparatus for determining blood volume



J. L.. NICKERSON 10d. 16, v194s.

' y IFPPAR'JUS FOR DETERMINING BLOOD VOLUME Filed Jan. 19, 1944 2 Sheets-Sheet l 25 n 1 vu cfm/km Oct. 16, 1945'. J. l.. NlcKERsoN APPARATUS FOR DETERMINING BLOOD VOLUME Filed Jan. 19, 1944 2 Sheets-Sheet 2 2.5. ...o mmiuz...

o e a l, T-m24 IN HUMAN SERUM l Fvg. 6.

s je J'om, L. Nickerson OPTICAL DENSITY (KON|GMARTENS SPEGTROPHOTOMETER) Patented Oct. 16, 1945 iif APPARATUS FOR DETER@ BEADOD V'IMIE .liohn Biester Nickerson, New York, N.

to United States of the Secretary of 'War Y., assigner erica, as represented by Application January i9, 1944i, Serial No. 518,911

(El. 8f4-1d) 7 Cialms.

This invention relates generally to photometry but more particularly to an instrument for determining blood volume.

One object of the invention is to provide a device by which a laboratory technician can easily and rapidly match the two elds of a photometer with respect to the control and dye tinted specimens and by direct reading obtain numerical values for the measurement of densities of such specimens.

Another object of the invention is to provide a' photometer including relatively adjustable series of filters having graduated optical densities by which the portion of the matching field, transmitting rays through the control medium, instead of being continuously variable, is changed in a series of individually distinct steps.

Another object of the invention is to provide an instrument for measuring plasma concentration which combines the featuresof portability, ruggedness, simplicity of operation, and accuracy, which make it suitable for either `ield work in the military service or laboratory work in a. base hospital. y

Still another object of the invention is to provide a photometer in which both halves of the f optical eld have the same tint so that no confusion as to color arises in matching intensities.

With -these and other objects in view, this invention consists in certain novel details of construction, combinaton and arrangement of parts to be more particularly hereinafter described and claimed.

Referring to the drawings, in which like parts are indicated by similar reference characters:

Figure l is a diagrammatic view showing the alignment of the various parts of the photometer;

Figure 2 is a top plan view of a rotatable lter disc provided with lters ranging in densities represented in hundredths from 0.00 to 0.09 inclusive; y

Figure 3 is a top plan view of a rotatable filter disc provided with Illters ranging in densities represented in tenths from 0.00 to 1.70;

Figure t is a chart showing spectral absorption curves;

Figure 5 is a chart showing curveswhich rep` resent transmission of the eyepiece lter with' plastic, human serum, and dog serum for various wave lengths with '1F-1824 dye in serums;

Figure 6 is a chart showing curves which represent the relationship between the scale reading of the instant photometer and the optical density scale reading of the Kohle-Martens spectrophotometer; and

' Figure 7 is an elevation of a serum cell showing details of construction of the container and stopper.

The instrument described herein was designed to meet the field requirements for the determination of blood volume by the procedure developed by Dr. Gregersen and in which the optical density oi the blue azo dye, designated as T4824, is used.v

Briey stated, the procedure may be outlined as follows:

If the patient has lost a substantial amount l of blood, the plasma injection should be equal to that lost. Too large an injection is asbad for the patient as not enough. Hence, the problem to be solved, insofar as this invention is concerned, is how much plasma has the patient lost.

By this method a known amount of blood is i'lrst withdrawn from the patient and a denite amount of dye injected, which diifuses through the blood stream in 5 to 10 minutes. Then another denite amount of blood is withdrawn, the plasma is separated from the dyed and yundyed samples and equal thicknesses of the two samples are compared colorimetrically to determine the amount of blood plasma lost. In order to facilitate the above-outlined procedure, particularly with respect to the operations of field units where speed of manipulation, accuracy, portability, and durability of apparatus are required, the instrument for comparison of the density of the dyed and normal blood plasma was devised. f

The instrument consists primarily of a light source adapted to direct two beams through equal thicknesses of two samples, one of which ccntains a definite amount of dye and the other being free of dye. The two beams of light pass to a single two-field matching ilter eyepiece where one-half of the circular field is illumihated by one beam and the other half by the other beam. By this arrangement the difference in the illumination on the two halves of the field is due solely to the light absorption by the dye, the plasma'in the two samples making equal change in each half of the filter.

The instrument is provided with a system of light-absorbing elements adapted to be moved into the path of the beam passing through the undyed sample. For this purpose a material, the light absorbing characteristics of which are the same as the dye, is employed, and therefore plastic nlters formed as strips or discs, which for a given range of the light spectrum have the same characteristics as the dye, are used..

To increase the speed and facilitate ease of lfeatures of portability,

2 operation of the rinstrument coaxial rotatable discs are provided. Within these discs are arranged a number of the aforesaid plastic slabs which are mounted adjacent the periphery thereof, so that they may be readily moved into the path of the beam which passes through the undyed sample. The slabs are ground to a definite graduated thickness so that the rotation of one disc will introduce into the path of the beam slabs calibrated in thicknesses of say 1 to 10, and the other disc will introduce into the beam slabs calibrated in thicknesses of say .l to 1. By turning the discs or wheels to introduce lters into the path of the beam, the combined densities of which are suiiicient to cause the same absorption as the dye, the two fields can accurately be matched, for the particular band of light spectrum, when viewed through the proper filter, and by calibrating the exact amount of plasma determined..

The instruments ordinarily used in measuring the plasma dye-concentration (e. g. the visual or photoelectric spectrophotometers, neutral wedge photometers, and Various types of photoelectric colorimeters) are satisfactory for laboratory purposes, but none ofthem combine the ruggedness, simplicity of operation and accuracy which would make7 them suitable for iield use.

In order to simplify the plasma dye determination and to eliminate some of the difficulties lost can be immediately encountered with other instruments, a portable photometer was designed in which the matching field, instead of being continuously variable is changed in a series of discrete and suitably related steps, as mentioned above.

The basis oi? the device, as set forth brieily above, consists in a series of colored plastic filters preferably formed as discs which are designated by the numerals I and I0' in Figures l, 2 and 3. These disc-shaped filters are arranged in two groups in circular openings II and |I' in the discs I2 and I2 which are rotatably mounted on a shaft I3, and retained thereon by the collars I4 and I4'.

The openings and II' in the discs |2 and I2 are stepped so as to form ledges Vi5 and I5' to support the circular filters which are held in place by rings I6 and I6', that may be glued or otherwise suitably attached to the internal circumference of the upper portion of the openings. The shaft I3 .is supported within a casing (not shown) which may be designed to house practically the entire device.

The groups of filters IIJ and I0 which are located respectively in the discs I2 and I2 are arranged in the order of their optical densities which increase in hundredths, from 0.00 to 0.09, in disc I2; and in tenths, from 0.30 to 1.70, in disc I2'.

Combinations of these filters in pairs, one lter for each group, makes it possible to determine optical densities from 0.30 to 1.70 insteps of 0.01, which is within the limit of intensity discrimination 'over most of the range.

The arrangement of the apparatus can be understood by examination of Figure 1. Two beams of light from a projection lamp II are directed by the mirrors I8, I8' through the ground glass screen I9 and the circular apertures 20 and 20' in plate 2|. One of the beams passes through a circular opening 22 in a supporting plate or stage 23, then through a glass cell 25 containing the clear control serum, thence in succession slabs by direct reference'to a table, the

through I0. one of the hundredth, and I0', one of the tenth plastic. filters, and flnallythrough a bi-prism 2G and a lens 21 to one-half of the field of filter 28 of beam passes through the opening 22' in plate 23, glass cell 25 of the same optical length .as 25 and lled with the dye-laden serum sample and then via the bi-prism 26, through lens 21' to the other half of the field of filter 28 of the eyepiece. If the basic `-unpigmented plastic has some residual color, it may be necessary to insert in the second beam two blocks of this material equal in thickness to in the iirst beam. With the particular plastic used here this is not necessary, for its transmission in the visible region of the spectrum is excellent. The eyepiece contains a filter with a transmission peak at 624 millimicrons enabling the intensities of the elds to be compared in a suitable and narrow spectral region.

Further details relating to the construction of the serum containers or cells 25 and 25' are shown in Figure '1.

These cells are tubular in form having a cylindrical body portion 35 which is attached to a circular disc-shaped base 36, the body and the base both being formed of transparent material.

The cylinder or body portion 35 is provided with a top or cover 31 which is drilled centrally to receive a transparent stopper 38. A flange 39 is provided at the upper end of the stopper to. limit its projection within the cylinder so that the distance between the bottom surface 40 of the stopper and the upper surface GI of the disc-shaped base 36 will be equal in all cells when the Stoppers are inserted into the covers to their full extent. Graduations on the cylinder may also be used to gauge the distance of insertion of the stopper so that bottom surface 40 thereof may be brought toa predetermined distance from the bottom 4| of the container.

The disc 36 is centered over the circular opening 22 or 22 latter with countersunk depressions adjacent the openings 22 and 22 and concentric therewith.

With the construction shown beams from the light source will always pass through an equal thickness of plasma on their paths between the disc and the stopper.

The rapid selection of the pairs of filters is attained by their arrangement on the two coaxial discs I2 and I2 which can be rotated by hand to bring any combination of a hundredth and a tenth density filter into the beam of the instrument. Tabs 30 and 30 marked with the hundredths and tenths are attached to the discs I2 and I2 at the position of the corresponding filters and by their juxtaposition at a convenient viewing point, the total optical density of the pair in the beam is shown as a numerical value, e. g. 1.54, where the pair consist of the 1.5 from the tenth range and the .04 from the hundredth range.

The exact centering of a filter in the beam automatically occurs when ball friction catches 3| and 3| each slip into one of the equally spaced depressions 32 and 32' in a steel plate 33 mounted on the shaft of the discs and retained rigidly thereon by the screw 34. The steel plate or disc I2 used with the hundredth range contains ten equally spaced depressions, and the plate or disc I2' for use with the tenth range has 16 depressions corresponding respectively to the 10 and 16 steps in those groups. The l16 plastic filters I0 of the tenth range comprise 15 tenths, 0.30 to the eyepiece 29. The other.

the two filters of plastic in the stage 23 by providing the with the corresponding colorless blank of the hundredth range enables the two beams to be initially matched in intensity thus constituting a zero setting. The-equalizingrof vthe fields in this situation is made by slight adjustments in the mirrors I8v and I8'. Once thisadjustment is obtained it seldom needs to be altered. A common diilculty in matching the fields appears when the halves of the field are not quite the same color. However, if both beams pass through identical materials this situation will not arise. Obviously this is not easy to arrange since one beam traverses the vblue dye in serum land the other passes through clear'serum and the. material of the color lter, One solution of this problem was attempted by constructing the color filters from gelatin iilms in which theblue dye itself was absorbed.l An exact correspondence between the beams was attained. This method was found to be impractical at the present 4time since iilters of this typewith exact optical densities could not be readily produced. Another approach could be the use of neutral tint filters, but with these the color differences can be quite disturbing, especially at the higher optical densities. It was found vthat sheets of a blue colored polymethyl methacrylate have a spectral absorption curve almost identical with that of the dye in serum between 600 and 680 ma. In Figure 4, curves A, B and C are the spectral absorption curves of samples of T1824 in human serum, of T-1824 in dog serum and of the plastic respectively adjusted to the same density at 624 ma. Since the eyepiece iilter 28 has a transmission illustrated by curve D it is clear that only light of wave lengths between 600 and 680 ma will reach the eye of the observer. In this range the spectral absorption curves A, B and C coincide rather well and this accounts for the fact that there is no perceptible color difference between the light transmitted through the plastic and that transmited through dyeserum samples.

The present transmission'of the eyepiece filter 28 in combination with the other materials in the beams is shown in Figure 5. The upper pair of curves indicate that a slight difference in spectral transmission exists between the plastic and the T-l824 in human serum. However, from a practical point of view, this difference produces no color variation between the halves of the field. The equivalence of the areas under these curves is an indication of the equality of total illumination on the iields. Similarly, two of the lower curves in Figure 5 show that the conditions of spectral transmission which provide good color matching and equality of illumination also hold for higher densities.

The matching of color and intensity having been attained. there remained the choice of a suitable numerical scale. The thicknesses of the plastic filters are proportional to the numbers on this scale. Since most spectrophotometers measure optical densities over a narrow spectral band (for the Konig-Martens spectrophotometer this band is '7 mit wide), and since the photometer "herein described has a transmission band 80 mit.

wide, the two types of instrument do Ynot transmit identical spectra. However, lit is" possible to adjust the plastic thicknesses for matching with T-1824 in human serum' to a scale which gives optical densities as measured in a Konig-Martens spectrophotometer. In Figure 6 the continuous line at 45 to the axes is the line of exact correspondence of the scales.y The circled points 'I'he dotted line in Figure 4 is for T-1824 in dog serum. The linearity is still excellent, but the subject photometer scale readings must be multiplied by 0.915 to provide the value as optical density at 624 mit. Examination of the dotted curve in Figure 4 shows that the transmission in the subject photometer is lower for T1824 in dog serum than for T1824 in human serum, althoughboth have the same transmission in a narrow spectral band at 624 ma. This difference in transmission accounts for the matching of the dye-dog serum with denser plastics (higher scale readings) thanthe dye-human serum. Preliminary tests have shown that'the scale of the instrument is also linear for T-1824 in cat and rabbit serum. Since the scale of the instant photometer is linear and essentially arbitrary, the instrument is suitable for independent calibration. Solutions of the dye in appropriate sera can be made up in accurate dilutions and read in 10 mm. cells. With these standardizations the dilution of subsequent samples may be computed from the scale readings.

The color stability of blue plastic material is extremely high with the appearance of fading only after several months exposure to summer sunlight. Since the component of sunlight responsible for this fading is the ultraviolet, it is apparent that the low intensity of ultraviolet light from an incandescent lamp, the etiicient filtering action of the ground glass diifusing screen, and suitable shielding of the filters from stray light combine to prevent color changes in the plastic.

'I'he plastic was fabricated in sheets of 1A inch thickness and in several optical densities. Out of these sheets disks of inch diameter were cut and the optical densities-measured on a Konig-Martens spectrophotometer at 624 ma, the peak of the absorption curve of the dye T-1824. From the thickness and optical density it was possible to compute the depth of plastic required to provide the exact density required in each of the filters. The disks were cut down in a lathe to about .002 inch greater than the computed thickness and then rubbed down to the exact dimension by the successive use of the finest sand paper, tripoli, rouge and finally a dry buii'er. This resulted in a brilliantly polished surface with the thickness correct to within .0003 inch. In general, however, it was not necessary to work closer than .001 inch and still limit the variations in optical density to less than .001.

Ihe advantages of this system are several. First, it enables a relatively inexperienced observer to match the two flelds of the photometer easily since the discrete steps aid in the Ijudgment; second, the numerical values of the optical densities on human sera are obtained directly; third, the measurements can be made rapidly; fourth, both halves of the field have the same tint so that no confusion as to color arises in the matching of intensities; and fifth, the apparatus can be made compact, portable and rugged, requiring little attention.

In order to describe more specifically the operation of the device, the method for the determination of the blood volume in normal subjects is set forth below.

The condition of the subject, namely, position, activity, and digestion, all iniluence the plasma .are samples experimentally determined on both instruments. The coincidence 'ly simpliiies the giving of dye and eliminates all calculations from the determination of plasma volume. These ampules contain exactly cc. of a solution of the dye designated as T-1824 which has been carefully standardized. The concentration (approximately 0.45 per cent in water) has been so adjusted that, when the solution is diluted 1:500 in human plasma or serum and read at 624 ma in mm. cells against an identical dye-free blank, its optical density is 0.8. Each dye ampule is wrapped in a package containing also a 10 cc. ampule of sterile saline which is needed in transferring the dye solution quantitatively to a syringe, as will be further explained.

With a 10 cc. syringe provided with a 20 or 2l gauge needle, 1A, cc. of a sterile saline is drawn up to wet the barrel and expel all air bubbles, leaving the needle as well as the tip of the syringe lled with saline. introduction of air, draw in all of the5 cc. of dye in the ampule. Follow this with another 1/2 cc. of saline in order to wash the dye in the needle back into the syringe. Detach the needle and expel any air bubbles that may be present. Do not attempt to rinse the ampule with saline. The amount of dye solution remaining in the ampule has been determined and allowance has been made for this in the illling of the ampule. Tests have shown that the overall error in this method of giving the dye is well within one per cent.

Without stasis collect 4 cc. of blood from the antecubital vein (dye-free sample). Detach the syringe from the needle (leaving the needle in the vein) and empty the blood into a 4 cc. hematocrit tube or 5 cc. serum tube containing 1 mgm. dry heparin to prevent clotting. Cork tube to prevent evaporation,

Through the needle already in the vein inject 5 cc. of the standard T1824 solution and note the time. Make sure that none of the dye escapes outside the vein. Rinse the syringe several times (3-5) with blood before withdrawing the needle.

Exactly 10 minutes after the dye injection, collectvanother 4 cc. sample of blood without stasis from the opposite antecubital vein or from the same vein in which the dye was given but peripheral to the site of the dye injection. Transfer this sample to a second 4 cc. hematocrit tube or 5 cc. serum tube containing dry heparin, and cork to prevent evaporation.

Determine the specinc gravity of the whole blood with the copper sulfate method (Phillips, Van Slyke, Dole et al., 1943). With a small hand centrifuge make a rapid separation of enough plasma for the dye determination. With some of this determine the specic gravity of the plasma. The relative erythrocyte volume as obtained by the conventional hematocrit method is calculated from the equation:

(blood sp. gr.) (plasma sp. gr.)

Being careful to avoid the assasve in which 1.0971 is the specific gravity or human red cells. Look for evidence of hemolysis in the supernatant plasma in both tubes (see below). The hematocrits and plasma protein values may be obtained also by reference to the charts provided by Phillips, Van Slyke et al. (1943) Alternative procedure: If a high-speed centrifuge is readily available, the hematocrit may be determined by centrifugation for 30 minutes at 3,000 R. l?. M. (radius l5 cm.). Provided the samples are properly taken without stasis, the hematocrits in the dye-free and dye-tinged samples should agree within one division.

Collect about 1 cc. of clear plasma from each blood sample with two narrow tipped pipettes (of the type described above). Transfer each plasma sample directly to the appropriate cell (22 and 22') as shown on the stage of the photometer as illustrated in Figure l.

View the matching fields of filter 2S through the eyepiece 29 of the photometer and then turn the upper disc or dial i2 clockwise until the field illuminated by rays passing through the undyed specimen or control appears slightly lighter in color than the eld illuminated by rays passing through the dye-tinted specimen. Then make a ne adjustment by turning the dial i 2 until the two elds match. Record the readings oi both dials, the added values of which represent the plasma dye concentration expressed in terms of optical density. From this value the total plasma volume is obtained by simply referring to the table (not shown) which is provided with the photometer.

The total blood volume is calculated from the equation:

Plasma volume cc. l hematocrit (D1X500) Vi=D2XVz in which; Q Di the density 0f the standard dye solution diluted 11500 in plasma V1 cc. oi? dye injected D2 density of dye in the circulating plasmarafter mixing has taken place V2 plasma volume.

total blood volume cc.=

draw V D2 The dye solution in the standard ampule has been made up to give a value for D1 of exactly 0.8. Since V1 is also a constant (5 cc.) and Dn is read directly on the photometer- Plasma volume i 00.5: 2000 0.8 50c I), or Smplv photometcr reading A wide range of plasma volumes (1150, to 6500) can be determined without any change in the procedure outlined above. If, however, the photometer reading exceeds 1.79 (plasma volume less than 1150) read the sample in 5 mm. depth instead of 10, multiply the reading by 2 and proceed as before in calculating the plasma volume. If

Hence, the plasma volume in cc.=

the reading approaches 0.3 (plasma volume greater than 6500), read the sample in 15 mm. depth and divide the value by 1.5. In this manner the range may be extended to include plasma volumes from 600 cc. up to 10,000 without altering the amount of dye injected.

The dose of T-1824 in the standard cc. ampule is in general adequate for determinations on adults. Unless given several times within a period of a few hours, this amount (approximately 20 mgms.) will not cause visible staining of the sublect. For routine determinations on small sub- Jects or on children it is advisable to reduce the dose. This can be done without sacrificing accuracy by reducing concentration of the dye solution ratherv than the volume injected.

Successful use of the dye method in measuring blood volume depends largely upon a knowledge of its limitations and of the manner in which variousconditions and technical errors may inval- .idate the results obtained. The circumstances un- -dyed blood specimens comprising a light source,

means for directing the rays from said source in parallel vertical beams, transparent cells provided with transparent stoppers. said cells being adapted to contain dyed and undyed plasma specimens and to interpose equal thicknesses of plasma in the path of said beams, supporting means adapted to retain said cells in an upright position in the path of said beams means for converging said beams to adjacent parallel paths, an eyepiece including a collimating lens and a two-field matching lter located in the path of said adjacent beams, a plurality of light absorbing elements of graduated densities circularly arranged in rotatable discs adapted for selectively interposing a combination of said elements in the path of said beam passing Athrough the undyed plasma specimen whereby the density of said specimen plus the added densities of said light absorbing elements may be compared with the density of the dyed plasma specimen by comparing the illumination of the fields of said two-held iilter to determine the dye-concentration of said dyed specimen.

2. An apparatus for determining blood volume of a patient by matching dyed and undyed specimens of plasma comprising a liglitsource, means for dividing the rays of said light source into two verticallyfdirected parallel beams, transparent cells for containing the dyed and undyed specimens of plasma, said cells being provided with transparent stoppers adapted to transmit said beams, means for supporting said cells and retaining them in positions to allow said beams to pass longitudinally through said stoppers therein, means for converging said beams to adjacent parallel paths, an eyepiece containing a collimating lens and a two iield matching filter, said filter being located within the path of said adjacent beams, rotatable discs mounted intermediate said converging means and said cells, iilters of progressively arranged densities circumferentially arranged in said discs, said filters being adapted t0 intersect the path of one of said beams intermediate the container of undyed plasma and said converging means, whereby the combined density of the cell containing undyed plasma plus the densities of the disc iilters may be matched optically with the combined density of the dyed plasma plus its containing cell, by rotating said discs until a combination of said filters ellects equal illumination of the fields of said matching filter.

3. An apparatus for determining blood volume of a patient by matching dyed and undyed specimens of plasma comprising a light source, reflecting means for dividing the rays or' said light source into two vertically directed parallel beams, transparent cells adapted tocontam dyed and undyed specimens of plasma, said cells being provided with transparent stoppers adapted to transmit said beams, means for supporting said cells and retaining them in positions to allow said beams to pass longitudinally through said stoppers therein, means Ior converging said beams to adlacent parallel paths, an eyepiece containing a collimating lens and a two neld matching nlter, said liner being located within the path of said aulacent beams, and rotatable discs mounted intermediate said converging means and said cells said discs being provided with filters of progressively arranged densities, said niters b'eing adapted to intersect the path of one or' said beams intermediate the container of undyed plasma and said conl verging means, whereby the combined density of the cell containing-undyed plasma plus the oeilsities of the disc Ii'lters may be matched optically with the density o1 the cell containing dyed plasma by rotating said discs until a combination of :filters intercepts the beam through said undyed specimen to eiiect equal illumination of the neids ofV said matching filter with the beam through said dyed specimen.

4. An apparatus for determining blood volume of alpatient by matching dyed and undyed specimens of plasma comprising a light source, means for dividing the rays of said light source into two vertically directed parallel beams, transparent cells for containing the dyed and undyed specimens of plasma, said cells being provided with transparent stoppers adapted to transmit said beams, a stage provided with two openings i'or supporting said cells and retaining them in positions to allow said beams to pass longitudinally through said stoppers therein, means for converging said beams to adjacent parallel paths, an eyepiece containing a collimating lens and a two iield matching filter adapted to transmit light waves within a predetermined wave band, said lter being located within the path of said adjacent beams, and rotatablel discs mounted intermediate said converging means and said containers said discs being provided with lters of progressively arranged densities, said filters being adapted to be selectively combined to intersect the path of one of s'aid beams intermediate the container of undyed plasma and said converging means by rotation of said discs, whereby the combined density of the cell of undyed plasma plus the densities of the disc filters may be matched optically with the density of 'the cell of dyed ',lasma by obtaining equal illumination of the fields of said matching filter.

5. An apparatus for determining blood volume of a patient by matching dyed and undyed specimens of plasma comprising a light source, means for dividing the rays of said light source into two vertically directed4 parallel beams, transparent cells for containing the dyed and undyed specimens of plasma, said cells being provided with transparent Stoppers adapted to transmit said beams, means comprising a stage for supporting said cells, said stage being provided with circular openings and countersunk depressions surrounding said openings for centering said cells in the path of said beams, means for converging said beams to adjacent parallel paths, an eyepiece containing a collimating lens and a two field matching filter, said filter being located within the path of said adjacent beams, and rotatable discs mounted intermediate said converging means and said containers, said discs being provided with filters of progressively arranged densities adapted to intersect the path of one of said beams inter-s mediate the cell of undyed plasma and said converging means whereby the combined density of the cell of undyed plasma plus the densities of the disc filters may be matched optically with the density of the container of dyed plasma by rotating said discs until equal illumination of the fields of the matching inter is btainee.

6. An apparatus for determining blood volume of a patient by the comparison of the optical densities of dyed and undyed blood specimens cornprising a light source, means for directing the rays from said source in parallel vertical beams, transparent cellsadapted to contain dyed and undyed plasma specimens, said cells being provided with transparent Stoppers adapted to project therein to within equal distances from the bottoms of the cells and thereby enclose equal depths of plasma therein, a horizontal stage provided with countersunk openings adapted to retain said cells in the paths of said beams, means for converging said beams to adjacent parallel paths, an eyepiece including a collimating lens and a two-field matching filter located in the paths of said adjacent beams, rotatably mounted discs, and a plurality of light absorbing elements of graduated densities arranged adjacent to the periphery of said discs, means for retaining said discs at predetermined angles of rotation to align selected combinations of said absorbing elements in the path of said beam passing through the asaaevs undyed plasma specimen whereby the density of said cell containing said specimen plus the added densities of said light absorbing elements may be matched with the density of the dyed plasma specimen. plus its containing cell, by rotating said discs until a combination oi light absorbing ele ments intercepts the beam through said undyed specimen to eiiect equal illumination of the lr iields.

7. An apparatus for determining blood volume of a patient by the comparison of the optical densities of dyed and undyed blood specimens com prising a light source, means for directing the rays from said source in parallel vertical beams, transparent cells adapted to contain dyed and undyed plasma specimens, means for vertically supporting said cells in the path o said beams, said cells being provided with transparent stoppers adapted to interpose equal thicknesses of plasma in the path oi 'said beams, means for converging said beams to adjacent parallel paths, an eyepiece including a collimating lens and a two-field matching iilter located in the path oi said adjacent beams, rotatably mounted discs, and means for equalizing the color of said iields, said means comprising a plurality of light absorbing elements formed of blue colored discs of polymethyl methacrylate and of graduated densities, arranged adjacent to the periphery of said discs, means for retaining said discs at predetermined angles of rotation to align selected combinations of said absorbing elements in the path of said beam passing through the undyed plasma specimen whereby the density of said specimen plus the density of the containing cell plus the added densities of said light absorbing elements, may be matched with the density of the dyed plasma specimen plus the density of its containing cell, by rotating said discs until a combination of light absorbing elements intercepts the beam through said undyed specimen to eiect equal illumination of the filter fields.

JOHN LESTER NICKERSQN. 

